Kendall 3142CRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521138827), received between Mar 9, 2021 and Mar 9, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Physical Resistance/Sticking” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 9, 2021Physical Resistance/Sticking; Physical Resistance/Sticking

  THE CUSTOMER REPORTED THAT THE TAPE WAS RIPPING THE SKIN OFF. ADDITIONAL INFORMATION WAS RECEIVED FROM THE CUSTOMER STATED THAT THE TAPE WAS USED ON A CAT. THERE WAS SOME SKIN IRRITATION OBSERVED WITH NO SIGNS OF INFECTION. THE CUSTOMER FURTHER STATED THAT AN OTC TOPICAL OINTMENT WAS USED AS A TREATMENT.

  Patient problems: Itching Sensation; Skin Tears

  MAUDE report 11448440 ↗